FDA 510(k)

MODEL A-8000 ULTRASONIC HANDPIECE CORD

K-Number: K862777 · 1986-08-11

ApplicantAdvanced Medical Technology, Inc.

Decision Date1986-08-11

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

MODEL A-8000 ULTRASONIC HANDPIECE CORD is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Technology, Inc.. It received FDA 510(k) clearance on 1986-08-11 under 510(k) number K862777. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL A-8000 ULTRASONIC HANDPIECE CORD?

MODEL A-8000 ULTRASONIC HANDPIECE CORD is a medical device that received FDA 510(k) clearance on 1986-08-11. The listed applicant is Advanced Medical Technology, Inc.. The 510(k) number is K862777.

When did MODEL A-8000 ULTRASONIC HANDPIECE CORD receive FDA 510(k) clearance?

MODEL A-8000 ULTRASONIC HANDPIECE CORD received FDA 510(k) clearance on 1986-08-11, under 510(k) number K862777.

Who is the listed applicant for MODEL A-8000 ULTRASONIC HANDPIECE CORD?

The FDA 510(k) record lists Advanced Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL A-8000 ULTRASONIC HANDPIECE CORD?

The FDA product code for MODEL A-8000 ULTRASONIC HANDPIECE CORD is HQC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.